Catheter

ABSTRACT

The present invention relates to a catheter that includes an elongate body having distal and proximal ends, the elongate body having at least one lumen therethrough, a distal portion of the elongate body having a perimeter. First and second retention members of the catheter are first and second retention members selectively disposed in either an insertion state or a retention state. In the insertion state, the first and second retention members form a distal body defining a central axis, the central axis being generally spaced apart from the perimeter of the distal portion of the elongate body, the distal body and elongate body insertable along a passageway of a mammal. In the retention state, the first and second retention members are selectively disposed in a spaced apart configuration to resist proximal movement of the catheter along the passage of the mammal.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of the U.S. National Stage designation of co-pending International Patent Application PCT/US03/31723 filed Oct. 2, 2003, which claims priority to U.S. application Ser. No. 10/261,662 filed Oct. 2, 2002, and the entire contents of these applications are expressly incorporated herein by reference thereto.

FIELD OF THE INVENTION

The present invention relates to catheters and to retention devices for removably retaining catheters within a body.

BACKGROUND OF THE INVENTION

Urinary catheters may be used to drain urine from the bladder of a catheterized individual. One known catheter, the Foley catheter, includes a balloon located near the tip of a tube sized to pass through the urethra. Once the tip is within the bladder, the balloon is filled with fluid to retain the tip in the bladder. Because the balloon must be bulky in order to retain the catheter tip, many patients experience discomfort when catheterized particularly if the balloon contacts the trigone, which is very sensitive. Moreover, the filled balloon may injure the patient if traumatically withdrawn from the bladder.

There is a need for a catheter that may be disposed within a bladder and retained without causing injury in the event of an unintentional withdrawal. Additionally, there is a need for a catheter that may be inserted and retained in a known orientation, thereby reducing contact with the trigone of the catheterized individual.

SUMMARY OF THE INVENTION

A first embodiment of the invention relates to a catheter, comprising an elongate body having distal and proximal ends, the elongate body having at least one lumen therethrough, a distal portion of the elongate body having a perimeter; first and second retention members, the first and second retention members being selectively disposed in either an insertion state or a retention state, wherein, in the insertion state, the first and second retention members forming a distal body defining a central axis, the central axis being generally spaced apart from the perimeter of the distal portion of the elongate body, the distal body and elongate body insertable along a passageway of a mammal; and in the retention state, the first and second retention members are selectively disposed in a spaced apart configuration to resist proximal movement of the catheter along the passage of the mammal. It should be understood that use of the word perimeter does not constrain the elongate body to have a circular cross section.

The first and second retention members may each include proximal and distal ends, the proximal ends rotatably associated with the distal end of the elongate body. The distal ends of the retention members may be free ends. The distal end of at least one of the first and second retention members may rotate about a rotation axis with respect to the distal end of the elongate body, the rotation axis generally disposed at a proximal end of the retention member. The distal end of each of the first and second retention members may rotate about a respective rotation axis with respect to the distal end of the elongate body, the rotation axes being generally disposed at respective proximal ends of the retention members.

A respective contour of the first and second retention members may remain substantially constant upon movement from the insertion state to the retention state.

The distal end of the catheter may include an opening to the passage, wherein the central axis of the distal portion of the elongate body intersects the opening. An inner surface of the passage may be substantially concentric with an outer surface of the elongate body.

When the first and second retention members are in the retention state, a distance between a distal extent of the retention members and an opening to the passage of the elongate body may be less than about 3 times a maximum radial dimension of the passage, wherein the distance is taken along the central axis of the distal portion of the elongate body.

The first and second retention members may move proximally upon moving from the insertion state to the retention state.

In the insertion position, a distal portion of the first retention member may extend beyond the second retention member, the distal portion of the first retention member having a substantially unbroken surface. When viewed along the central axis of the substantially distal body, the substantially unbroken surface of the first retention member may obscure at least a portion of the second retention member.

The catheter may further comprising a linkage, wherein the first and second retention members are actuated via the linkage. The linkage may comprise a linkage member, the linkage member being rotatably associated with the first retention member and slidably associated with the second retention member. The second retention member may include a stop, which, in the retention state, releasably accommodates an end of the linkage member thereby inhibiting the retention members from returning to the insertion position. The stop and the end of the linkage member are configured to dissociate in response to a predetermined proximal force so that the retention members may return to the insertion state.

The linkage may include first and second linkage members having respective first and second ends, wherein the first end of the first linkage member is rotatably associated with the first retention member, the first end of the second linkage member is rotatably associated with the second retention member, and the respective second ends of the first and second linkage members are rotatably associated with one another.

The linkage may comprise first and second linkage members, the first and second linkage members rotatable with respect to one another about a rotation axis, wherein, as the first and second retention members move between the insertion state and the retention state, the rotation axis translates substantially along the central axis of the distal body. A distal extent of at least one of the first and second retention members may be greater than a distal extent of the linkage.

The linkage may include a linkage member having first and second linkage member ends, a first end of the linkage member is slidably and rotatably associated with the first retention member and the second linkage member end is slidably and rotatably associated with the second retention member.

The catheter may include a flexible enclosure, wherein movement from the insertion state to the retention state is actuated by expansion of the flexible enclosure.

A radial extent of at least one of the first and second retention members may be at least about as great as a length of the retention member.

The distal body may bifurcate upon moving from the insertion state to the retention state.

The catheter may comprise a proximal portion having at least one spatial marker indicative of an orientation of the first and second retention members. At least one spatial marker may be indicative of whether the retention members are aligned with a coronal plane of a human catheterized with the catheter.

The passage may be a urethra. The mammal may be a human.

Another embodiment of the invention relates to a method for catheterizing a mammal, comprising, providing a catheter comprising an elongate body having distal and proximal ends, the elongate body having at least one lumen therethrough, a distal portion of the elongate body having a perimeter; first and second retention members, the first and second retention members being selectively disposed in either an insertion state or a retention state, wherein, in the insertion state, the first and second retention members forming a distal body defining a central axis, the central axis being generally spaced apart from the perimeter of the distal portion of the elongate body, the distal body and elongate body insertable along a passageway of a mammal; and in the retention state, the first and second retention members are selectively disposed in a spaced apart configuration to resist proximal movement of the catheter along the passage of the mammal; inserting the catheter along a passageway of the mammal until first and second retention members of the catheter enter a cavity of the mammal; and moving the retention members from an insertion state to a retention state, whereby the first and second retention members are removably retained within the cavity.

Still another embodiment of the present invention relates to a urethral catheter for catheterizing a bladder of a human having a coronal plane. The urethral catheter comprises an elongate body having a distal portion and a proximal portion, the elongate body having a passage therealong; first and second retention members movably associated with the distal portion of the elongate body, the first and second retention member movable between an insertion state and a retention state, wherein, in the retention state the first and second retention members extend radially and substantially along a single plane from the elongate body; and the proximal portion of the elongate body includes at least one spatial marker indicative of the whether the first and second retention members are generally aligned with the coronal plane of the human when the first and second retention members are in the bladder of the human.

The first and second retention members may include respective distal outer surfaces, and wherein the respective distal outer surfaces define an angle of at least about 80 degrees with respect to a central axis of the distal portion of the elongate body.

Yet another embodiment of the present invention relates to a urinary catheter retention device for insertion along a urethra into a bladder of a human to releasably retain a passage of an elongate body in fluid communication with the bladder, the retention device comprising a base operably securable to an end of the elongate body; first and second retention members movably associated with the base and having respective free distal ends, the free distal ends of the retention members movable between an insertion state and a retention state, wherein, in the insertion state, the first and second retention members cooperate to form a body, the body being insertable along the urethra; and in the retention state, the free distal ends are spaced apart from one another to resist proximal movement of the elongate body along the passage of the mammal.

Yet another embodiment of the invention relates to a urethral catheter, comprising an elongate body, the elongate body having at least one lumen therethrough; a first retention member, the first retention having first and second ends and being selectively disposed in either an insertion state or a retention state, wherein, in the insertion state, the first and second ends of the retention member are generally aligned with the elongate body so that at least a portion of the catheter is insertable along a urethra of a mammal; and in the retention state, the first and second ends of the retention member are spaced apart from the elongate body to resist proximal movement of the retention member along the urethra of the mammal.

A generally medial portion of the retention member may be rotatably associated with the catheter.

The catheter may include at least one tension member that urges a generally medial portion of the retention member toward a distal end of the catheter.

An axial distance between the generally medial portion of the retention member and a distal end of the elongate body may decrease by at least about one half upon moving from the insertion state to the retention state.

Still another embodiment of the invention relates to a urethral catheter, comprising an elongate body having a distal end and a proximal end and at least one lumen therethrough; at least a first retention member, the at least first retention member being generally associated with the distal end of the elongate body and selectively disposed in at least an insertion state and a retention state, wherein, in the insertion state, the at least first retention member is generally aligned with the elongate body and insertable along a urethra of a mammal; and, in the retention state, at least a portion of the at least first retention member is radially spaced apart from the elongate body, wherein, upon the application of a force of less than about 10 Newtons directed generally proximally along the elongate body, the at least one retention member resists proximal movement of the catheter along the urethra and, upon the application of a force of less than about 25 Newtons directed generally proximally along the elongate body, the at least one retention member returns to an insertion state to permit withdrawal of the catheter along the urethra.

Upon the application of a force of less than about 20 Newtons directed generally proximally along the elongate body, the at least one retention member may return to an insertion state to permit withdrawal of the catheter along the urethra.

Upon the application of a force of less than about 15 Newtons directed generally proximally along the elongate body, the at least one retention member may return to an insertion state to permit withdrawal of the catheter along the urethra.

Another embodiment of the invention relates to a urinary drainage catheter, comprising an elongate body comprising a distal portion, a proximal portion, and first and second separate passages therealong. The catheter may include a distal balloon operatively associated with the distal portion of the elongate body, and, optionally, a proximal balloon operatively associated with the proximal portion of the elongate body, the distal and proximal balloons preferably being in hydraulic communication with one another, such as via the second passage, wherein an expansion of one of the balloons accompanies a contraction of the other of the balloons.

The distal portion of the elongate body may be disposed in fluid communication with a bladder of a mammal, the first passage allows fluid to exit the bladder.

The urinary drainage catheter may be provided within a sealed enclosure comprising the urinary drainage catheter. The catheter is sterile and at least one of the distal and proximal balloons may comprise a fluid, such as an aqueous liquid.

Another embodiment of the present invention relates to a urinary drainage catheter, comprising an elongate member comprising a distal portion, a proximal portion, and a urinary drainage passage therealong. The catheter may have a hydraulically actuated retention mechanism operatively associated with the distal end of the elongate member, the hydraulically actuated retention mechanism preferably comprising an actuation fluid and at least one retention member rotatably associated with the distal portion of the elongate body. The retention member preferably (i) being free of the actuation fluid and, optionally, (ii) being hydraulically rotatable between an insertion state and a retention state, the retention state being configured to resist withdrawal of the catheter when the retention member is deployed in the retention state within the bladder, the actuation fluid preferably not entering the retention member upon actuation to the retention state.

Another embodiment of the invention relates to a urinary drainage catheter for draining fluid from a bladder of a catheterized mammal. The catheter may comprise an elongate body, comprising a distal portion, a proximal portion, and first and second separate passages extending therealong. The catheter may include a distal enclosure operatively associated with the distal portion of the elongate body and having an insertion state and a retention state, the distal enclosure preferably being inflatable from the insertion state to the retention state upon the introduction of an actuation fluid thereto and collapsible from the retention state to the insertion state upon the exit of at least some of the actuation fluid therefrom. When the distal enclosure is in the retention state within the bladder, the distal enclosure preferably resists withdrawal of the distal portion of the catheter along the urethra and the first passage facilitates drainage of fluid from the bladder.

The catheter may include a fluid release mechanism operatively associated with the proximal portion of the elongate body, the distal enclosure being in hydraulic communication with the fluid release mechanism via the second passage, wherein, when the catheter is subjected to a traumatic withdrawing force directed substantially along the urethra, the release mechanism operates to allow actuation fluid to exit the second passage, whereupon the distal enclosure collapses to the insertion state.

The fluid release mechanism may be external to the urethra when the distal enclosure is disposed within the bladder. The fluid release mechanism may comprise an expandable enclosure and operation of the fluid release mechanism comprises introduction of fluid to the expandable enclosure from the second passage. The expandable enclosure may comprise an expandable balloon formed of elastic material. The distal enclosure may comprise an expandable balloon formed of elastic material. The expandable enclosure may be an expandable sack formed of flexible material.

The fluid release mechanism may comprise a membrane and actuation of the fluid release mechanism may comprise at least one of an increase in an area of the membrane and a rupture of the membrane. The membrane may have a thickness less than a thickness of the second passage adjacent the membrane. The fluid release mechanism may comprise a relief valve, such as a poppet relief valve.

Another embodiment of the present invention relates to a urinary drainage catheter for draining fluid from a bladder of a mammal, comprising (i) an elongate body comprising a distal portion, a proximal portion, and a first passage extending therealong, the passage comprising a distal opening and a proximal opening, and (ii) a distal enclosure operatively associated with the distal portion of the elongate body and configurable in an insertion state and a retention state. When the distal enclosure is in the insertion state, at least the distal portion of the catheter is preferably insertable along a urethra of the mammal at least until at least a portion of the distal enclosure resides within the bladder. When the distal enclosure is in the retention state and at least partially resident within the bladder, the distal enclosure preferably resists withdrawal of at least the distal portion of the catheter along the urethra. The distal enclosure may expand from the insertion state to the retention state upon the entry of fluid thereto and contract from the retention state to the insertion state upon the exit of fluid therefrom.

The catheter may include a proximal flexible fluid enclosure (proximal enclosure) in fluidic communication with the distal enclosure, wherein (a) at least a portion of at least one of the proximal enclosure and the proximal opening of the passage preferably resides external to the urethra when the distal enclosure is in the retention state and resident within the bladder, the passage providing drainage of fluid from the bladder, and (b) exit of fluid from the proximal enclosure actuates expansion of the distal enclosure from the insertion state to the retention state and entry of fluid into the proximal enclosure may accompany contraction of the distal enclosure from the retention state to the insertion state.

The proximal enclosure may be formed of an elastic material. The proximal enclosure may comprise a balloon. The proximal enclosure may comprise a flexible sack.

A proximal portion of the elongate body may comprise an at least partially circumferential collar, the collar movable longitudinally along the elongate body, wherein, when the distal enclosure is in the insertion state, the collar may be moved over the proximal enclosure to allow the introduction of fluid to the distal enclosure without substantial expansion of the proximal enclosure.

The proximal enclosure, in the insertion state, may comprise a maximum radial dimension at least 1.5 times greater, such as at least 2.5 times greater, or at least 3.0 times greater than a maximum radial dimension of a distal portion of the elongate body.

The distal and proximal enclosures may be connected by a second passage along which fluid may pass unobstructed between the enclosures. The first and second passages may be are separate from one another.

The distal enclosure may comprise at least one of an elastic material and flexible material. The distal enclosure may comprise a balloon.

The proximal enclosure may comprise a balloon.

The distal enclosure may comprise a flexible sack.

The distal enclosure may comprise an aqueous liquid and, optionally, expansion and contraction of the distal enclosure respectively comprise introduction and removal of the aqueous liquid therefrom. The aqueous liquid may be saline solution.

When distal enclosure is in the retention state and resident within the bladder, a withdrawing force of greater than 10 lbs directed along the urethra and applied to the proximal portion of the catheter may actuate collapse of the distal enclosure whereby the catheter may withdraw from the urethra without substantial injury to the mammal. The mammal may be a human.

The catheter may be provided within a sealed enclosure comprising the urinary drainage catheter.

Another embodiment of the invention relates to a method for catheterizing a mammal, comprising providing a catheter, the catheter comprising an elongate body comprising a distal portion, a proximal portion, a distal enclosure operatively associated with the distal portion of the elongate body, and a proximal enclosure having at least one flexible wall, the proximal enclosure being in fluidic communication with the distal enclosure.

The distal portion of the elongate body may be passed along at least a portion of the urethra of the mammal, at least a portion of the proximal enclosure remaining outside the urethra. Fluid may be introduced to the distal enclosure by applying pressure to the flexible wall of the proximal enclosure whereupon fluid exits the proximal enclosure and fluid enters and expands the distal enclosure within the bladder of the mammal, wherein the expanded distal enclosure resists withdrawal of the catheter along the urethra of the mammal.

The proximal enclosure may comprise at least one of a balloon and a flexible sack and applying pressure to the flexible wall comprises squeezing the at least one of the balloon and flexible sack.

The catheter may be a urinary drainage catheter comprising at least one drainage passage and, upon expansion of the distal enclosure, a distal opening of the at least one drainage passage may be disposed in fluidic communication with the bladder.

The step of providing a catheter may comprise opening a sealed enclosure enclosing the catheter, wherein, when the catheter is present within the sealed enclosure, at least one of the proximal and distal enclosures may comprise an amount of liquid sufficient to expand the distal enclosure by an amount sufficient to resist withdrawal of the catheter from the urethra

Another embodiment of the invention relates to a urinary drainage catheter, comprising an elongate member comprising a distal portion, a proximal portion, an actuation passage, and a urinary drainage passage, wherein the actuation passage and urinary drainage passage are separate from one another. The catheter may include an hydraulically actuated retention mechanism operatively associated with the distal portion of the elongate member, the hydraulically actuated retention mechanism being deployable in an insertion state and a retention state, the retention state being configured to resist withdrawal of the catheter when the retention mechanism is deployed within the bladder. The catheter may include a proximal enclosure comprising at least one flexible wall and being in fluidic communication via the actuation passage with the hydraulically actuated retention mechanism, wherein exit of fluid from the proximal reservoir actuates movement of the retention mechanism from the insertion state to the retention state and entry of fluid to the proximal enclosure accompanies movement of the retention mechanism from the retention state to the insertion state.

Another embodiment of the invention relates to an apparatus for use in catheterizing a mammal, the apparatus comprising a sealed enclosure enclosing at least a sterile urinary drainage catheter, the catheter comprising an elongate body comprising a distal portion, a proximal portion, and a passage therealong, a hydraulically actuated retention mechanism operatively associated with the distal portion of the elongate body, the retention mechanism comprising a distal enclosure and having an insertion state and a retention state, wherein, when the retention mechanism is in the insertion state, at least the distal portion of the elongate body is insertable along the urethra of the mammal, and when the retention mechanism is in the retention state, the retention mechanism resists withdrawal of at least the distal portion of the elongate body along the urethra, a proximal enclosure operatively associated with the proximal portion of the elongate body, the proximal enclosure comprising at least one flexible wall and being in fluid communication with the retention mechanism, wherein at least one of the distal enclosure and the proximal enclosure comprise a fluid, wherein exit of fluid from the proximal enclosure and entry of fluid to the distal enclosure actuate movement of the retention mechanism from the insertion state to the retention state and entry of fluid to the proximal enclosure and exit of fluid from the distal enclosure actuate movement of the retention mechanism from the retention state to the insertion state.

The proximal enclosure may comprise a liquid when the catheter is enclosed within the sealed enclosure. The liquid may be aqueous. The distal enclosure and the proximal enclosure may be a closed system.

The retention mechanism may comprise a first retention member, the first retention member preferably being rotatatable with respect to the distal portion of the elongate body and wherein movement of the retention mechanism from the insertion state to the retention state comprises rotation of the first retention member with respect to the distal portion of the elongate body.

The retention mechanism may comprise a second retention member, the second retention member preferably being rotatatable with respect to the distal portion of the elongate body and wherein movement of the retention mechanism from the insertion state to the retention state comprises rotation of the second retention member with respect to the distal portion of the elongate body.

Another embodiment of the invention relates to a urinary drainage catheter for catheterizing a mammal, comprising an elongate body comprising a distal portion, a proximal portion, and a urinary drainage passage therealong and an actuation passage therealong, a hydraulically actuated retention mechanism operatively associated with the distal portion of the elongate body, the retention mechanism comprising a distal enclosure and having an insertion state and a retention state, wherein when the retention mechanism is in the insertion state, at least the distal portion of the elongate body is insertable along the urethra of the mammal, when the retention mechanism is in the retention state within the bladder of the mammal, the retention mechanism resists withdrawal of at least the distal portion of the elongate body along the urethra, and movement of the retention mechanism from the insertion state to the retention state is actuated by entry of fluid to the distal enclosure and movement of the retention mechanism from the retention state to the insertion state comprises exit of fluid from the distal enclosure along the actuation passage, and a fluid release mechanism in fluid communication with the distal enclosure along the actuation passage, wherein, when the retention mechanism is disposed in the retention state within the bladder of the mammal, the fluid release mechanism is configured to allow fluid to exit the distal enclosure upon the application of a withdrawal force directed generally along the urethra, whereupon the retention mechanism returns to the insertion state and the catheter may withdraw along the urethra without substantial injury to the mammal.

The fluid release mechanism may comprise a membrane and actuation of the fluid release mechanism comprises at least one of an increase in the area of the membrane and rupture of the membrane. The membrane may have a thickness less than a thickness of the actuation passage adjacent the membrane. The membrane may be disposed external to the urethra when the retention mechanism is within the bladder.

The fluid release mechanism may comprise a release valve. The valve may be a poppet type relief valve.

The fluid release mechanism may comprise an expandable enclosure, fluid preferably entering and expanding the expandable enclosure upon actuation of the fluid release mechanism.

BRIEF DESCRIPTION OF THE DRAWINGS

The present invention is discussed below with reference to the drawings, in which:

FIG. 1 shows a first embodiment of a catheter of the present invention, the catheter being configured in an insertion state;

FIG. 2 shows the catheter of FIG. 1, the catheter being configured in an retention state;

FIG. 3 shows a distal portion of the catheter of FIG. 1 in an insertion state;

FIG. 4 shows a perspective of a distal portion of the catheter of FIG. 1, the catheter being configured in a retention state;

FIG. 5 shows a side view of the catheter of FIG. 4;

FIG. 6 shows an axial view of the catheter of FIG. 1, the catheter being configured in a retention state in a bladder of a human;

FIG. 7 shows a perspective view of the catheter of FIG. 1, the catheter being configured in a second retention state;

FIG. 8 shows a perspective view of the catheter of FIG. 1, the catheter being configured in a third retention state;

FIG. 9 shows a side view of distal portion of a second embodiment of a catheter of the present invention, the catheter being configured in an insertion state;

FIG. 10 shows a perspective view of a distal portion of the catheter of FIG. 9, the catheter being configured in a retention state;

FIG. 11 shows a cross-sectional side view of a distal portion of a third embodiment of a catheter of the invention, the catheter being configured in an insertion state;

FIG. 12 shows a cross-sectional side view of a distal portion of the catheter of FIG. 11, the catheter being configured in a retention state;

FIG. 13 shows a side view of a distal portion of a fourth embodiment of a catheter of the invention, the catheter being configured in an insertion state;

FIG. 14 shows a side view of a distal portion of the catheter of FIG. 13, the catheter being configured in a retention state;

FIG. 15 shows a perspective view of an elongate body of the catheter of FIG. 13, retention members of the catheter not being shown;

FIG. 16 shows a fifth embodiment of a catheter of the present invention, the catheter being configured in an insertion state;

FIG. 17 shows side view of a distal portion of the catheter of FIG. 16, with the catheter being configured in a retention state;

FIG. 18 shows an embodiment of a catheter retention device of the present invention, the retention device being configured in an insertion state;

FIG. 19 shows a side view of the catheter retention device of FIG. 18, the catheter device being configured in a retention state;

FIG. 20 shows a perspective view of the catheter retention device of FIG. 18, the catheter being configured in a retention state;

FIGS. 21 and 22 show a sixth embodiment of a catheter of the present invention, with catheter being configured in an insertion state;

FIGS. 23 and 24 show the catheter of FIGS. 21 and 22 being configured in a retention state;

FIGS. 25 and 26 show a seventh embodiment of a catheter of the invention, with the catheter being respectively configured in an insertion state and a retention state; and

FIG. 27 shows an eighth embodiment of a catheter of the invention, with the catheter being configured in an insertion state;

FIGS. 28 and 29 show the catheter of FIG. 27 but being configured in a retention state;

FIGS. 30A and 30B show an embodiment of a catheter retention device of the invention, the catheter being respectively configured in an insertion state and a retention state, a hydraulic actuation device not being shown;

FIG. 31A shows a perspective view of the catheter retention device of FIGS. 30A and 30B;

FIGS. 31B-31C show perspective views of the catheter retention device of FIGS. 30A and 30B, a hydraulic actuation device being shown; and

FIG. 32 shows a catheter comprising the catheter retention device of FIGS. 30A to 31C.

DETAILED DESCRIPTION OF THE INVENTION

Referring to FIGS. 1 and 2, a catheter 20 of the present invention is shown including an elongate body 22. Catheter 20 has a proximal portion 24 and a distal portion 26. The catheter 20 may be configured in at least either an insertion state or a retention state, as shown in FIGS. 1 and 2, respectively. In the insertion state, catheter 20 is insertable along a passageway or lumen of a mammal until at least a portion of distal portion 26 resides within a cavity of the mammal. In the insertion state, catheter 20 may be removed along the passageway or lumen of a mammal without causing injury thereto. Distal portion 26 preferably includes at least two retention members 28, 30 which are movably associated with catheter 20. In the retention state shown in FIG. 2, at least a portion of at least one of retention members 28, 30 is radially extended, thereby resisting proximal movement of catheter 20 along the passage. In a preferred embodiment, both retention members 28, 30 are radially extended in a retention state.

Catheter 20 has at least one retention member and may have 2, 3, 4 or even more retention members. A preferred embodiment of catheter 20 has 2 retention members that retain the catheter in a body cavity. Movement of retention members in accordance with the present invention from the insertion state to the retention state is an opening movement. In a two-retention member catheter, the preferred retention member opening is a bifurcation. Movement of retention members from the retention state to the insertion state is a closing movement. For example, an operator may actuate a closing movement of radially extending retention members 28, 30 of catheter 20 so that the catheter returns to the insertion state allowing the catheter to be withdrawn along a passageway without causing injury to a catheterized mammal.

With respect to the anatomy of a mammal catheterized with catheter 20, the term distal refers to a location that is farther along the passageway from an exterior opening thereof than is another location disposed closer to the exterior of the passageway. For example, catheter 20 may be inserted along the urethra of a human so that retention members 28, 30 are positioned within the bladder of the human. Upon such an insertion, the bladder and retention members 28, 30 are distal to the external opening of the urethra. With respect to catheter 20, the term distal refers to locations closer to a distal end 36 thereof than to proximal portion 24.

Referring to FIG. 3, first and second retention members 28, 30 cooperate in the insertion state to form a distal body 34, which is shaped to allow catheter 20 to be inserted along a passageway. Distal body 34 may be substantially cylindrical, prolate, conical, wedged, spherical, or have another configuration suitable to allow the catheter to pass along the respective passageway. During the insertion, the distal body 34 is distal to elongate body 22. Thus, insertion of catheter 20 along a passage may also be facilitated by the shape of distal end 36 of distal body 34. Respective retention member distal ends 33, 35 preferably cooperate to form a single substantially blunt surface at distal end 36. Other than distal body 34, distal portion 26 of catheter 20 is preferably free of distally extending projections, such as those that may engage or interfere with portions of the passage as the catheter is inserted therealong.

Distal body 34 defines a distal body axis a₁, which is central to a perimeter p₁ of distal body 34, as shown in FIG. 3. A distal portion 27 of elongate body 22 defines a distal portion axis a₂, which is central to a perimeter p₂ a of distal portion 27 of elongate body 22. Distal body axis a₁ is preferably spaced apart from perimeter p₂. In a preferred embodiment, distal body axis a₁ is central to perimeter p₂. Distal body axis a₁ may be aligned with distal portion axis a₂ of distal portion 27 of elongate body 22. It should be understood that, because elongate body 22 may be formed of a flexible material, the relative alignment of distal body axis a₁ and distal portion axis a₂ may vary. When, however, catheter 20 is straightened so that perimeters p₁, p₂ are parallel to one another, axes a₁, a₂ are preferably alignable, as seen in FIGS. 1 and 3.

Referring to FIGS. 4-6, the radial extent of first and second retention members 28, 30 increases upon moving from the insertion state to the retention state so that catheter 20 resists proximal movement along a passage when the retention members are within a cavity. Thus, distal retention member ends 33, 35 are spaced apart and retention members 28, 30 no longer cooperate to form distal body 34. In the retention state, a respective radial extent d₁ of at least one and preferably both retention members 28, 30 is preferably at least about as great and more preferably greater than a respective retention member length l₁. Radial extent d₁ is the distance from the maximum radial extent of an end of a retention member to central axis a₂. For example, the radial extent d₁ of a retention member may be at least about 90%, at least about 100%, or at least about 110% of the length l₁ of the retention member. Of course, the radial extent of retention members of catheters of the invention may be different, for example, if either of retention members 28, 30 is rotated farther out from central axis a₂. Similarly, the lengths of retention members may be different.

The opening motion of the retention members 28, 30 preferably does not involve bending of respective medial portions 53, 55 of the retention members. Retention members 28, 30 preferably do not compress, such as along axis a₁, upon opening. Thus, the respective lengths of retention members 28, 30 are preferably substantially the same in both the insertion and retention states.

A width w₁ of retention members 28, 30 may be substantially constant as a function of radial distance along the length thereof. Alternatively, w₁ may vary as a function of distance from central axis a₁. For example, a width of the retention members may initially increase with radial distance perhaps decreasing toward distal ends of the retention members so that they have a shape that is petaloid, prolate, spheroid, or similar. In the insertion state, the distal body formed by the cooperation of such petaloid or prolate retention members may form a waist or narrower region that is disposed proximal to a distal end of the distal body. Other exemplary retention members have a maximum width at proximal ends thereof and taper to a smaller width at their distal ends.

A lumen 32 runs substantially along an interior length of elongate body 22. When retention members 28, 30 are within a cavity of a mammal, lumen 32 may be in fluid communication with the cavity so that fluid may pass along the lumen between an exterior of the mammal and the cavity. Preferably, fluid may exit the cavity via lumen 32. A distal opening 38, which is preferably disposed at a distal end 40 of elongate body 22, allows fluid to enter lumen 32. For example, urine may exit a bladder of a catheterized mammal. Proximal portion 24, which preferably remains at least partially exposed upon catheterization with catheter 20, may be configured to operatively connect with a drainage system or reservoir so that fluid exiting the cavity may be disposed of or collected.

In the retention state, as seen in FIG. 5, a location of a maximum distal extent of catheter 20 is preferably spaced apart from axis a₂ of the distal portion 27 of elongate body 22. A radial distance between axis a₂ and a portion defining a maximum distal extent of the catheter may be at least twice a maximum radial dimension of distal portion 27, such as at least three or four times a diameter thereof. For example, a location of maximum distal extent may be determined by respective distal ends 33, 35 of retention members 28, 30.

In the retention state, a distance d₂ between distal opening 38 and the maximum distal extent of catheter 20 is preferably less than about 6 times, such as less than about 4 times greater than the diameter d₃ of distal portion 27 of elongate body 22.

Distal opening 38 is preferably intersected by central axis a₂ of distal portion 27 of elongate body 22. Lumen 32 is preferably concentric with elongate body 22. Lumen 32 may be the only lumen passing along the length of the elongate body 22 between the proximal 24 and distal 27 portions thereof. Therefore, the capacity of the lumen 32 to conduct fluid is increased as compared to a catheter having more than one lumen extending therealong.

Referring back to FIG. 4 and also to FIGS. 7 and 8, respective distal ends 33, 35 of retention members 28, 30 rotate with respect to elongate body 22 during movement between the insertion and retention states. The distal ends 33, 35 preferably rotate about respective rotation axes a₃, a₄, which axes are preferably disposed at or adjacent respective proximal ends 37, 39 of retention members 28, 30. The retention members 28, 30 preferably open and close without bending along their lengths other than any bending that may occur at or adjacent their proximal ends 37, 39. The rotatable association is via respective first and second flexible connections 42, 44, which are preferably capable of repeated bending without damage. The rotatable association of retention members 28, 30 may also be accomplished by other elements, such as pivots or hinges, by which at least one of retention members 28, 30 may rotate with respect to catheter 20. The flexible connections may be secured to catheter 20 using, for example, at least one of friction, adhesives or ultrasonic welding. Alternatively, retention members 28, 30 may be integral with distal portion 27 of elongate body 22 of catheter 20.

Referring back to FIG. 5, respective proximal outer surfaces 58, 60 of retention members 28, 30 define, in the retention state, an angle θ₁ of at least about 65 degrees, preferably at least about 75 degrees, and most preferably at least about 80 degrees with respect to central axis θ₁ of distal body 34. Angle θ₁ is preferably less than about 115 degrees, such as less than about 100 degrees or even less than about 95 degrees. Thus, with angle θ₁ at least about 75 degrees, the retention members 28, 30 proximally extending and elongate body 22 may be said to define a “T-shape.” One or both of portions 58, 60 may be distal to portions 37, 39 when the retention members are in a retention state.

As best seen in FIGS. 6 and 7, the first and second retention members 28, 30 may be actuated by a linkage 46. Upon a first actuation motion of linkage 46, retention members 28, 30 move from the insertion state to the retention state. Upon a second actuation motion of linkage 46, retention members 28, 30 move from the retention state to the insertion state.

Linkage 46 includes first and second linkage portions 52, 54 that rotate with respect to one another about a rotation axis a₅ at a rotatable connection 56, as seen in FIG. 6. Linkage portions 52, 54 may be of unitary construction or may be formed of separate portions connected by rotatable connection 56. Linkage portions 52, 54 have a length l₂, which is less than about 75%, such as less than about 60%, as long as length l₁ of retention members 28, 30.

Upon actuation of linkage 46, rotatable connection 56 translates generally linearly along central axis a₁ of distal body 34. Rotatable connection 56 may be a pivot having a pivot pin 58 centered upon rotation axis a₅. A rotatable connection may instead be formed of a flexible connection that allows the first and second linkage portions 52, 54 to rotate with respect to one another. A rotatable connection may also be a connection in which a portion of one of the linkage members rotates within a portion of the other linkage member. A socket joint in which a convex portion, such as a ball-like portion, of one linkage member rotates within a concave portion, such as a socket, of the other linkage member is an example of such a connection.

First and second linkage portions 52, 54 are rotatably associated with first and second retention members 28, 30, respectively. Upon actuation of linkage 46, linkage portion 52 rotates with respect to retention member 28 about a rotation axis a₆ via a rotatable connection 62; linkage portion 54 rotates with respect to retention member 30 about a rotation axis a₇ via a rotatable connection 64. Thus, one embodiment of the linkage may include 3 rotatable connections. Rotatable connections 62, 64 are pivots having respective pivot pins 66, 68 centered about respective rotation axes a₆, a₇. Alternatively, linkage portions 52, 54 may be rotatably associated with respective retention members 28, 30 via flexible connections or socket joints.

In the retention state, a radial distance d₄ between one and preferably both of rotatable connections 62, 64 and central axis a₁ of distal body 34 is preferably less than the respective radial extent d₁ of the one or both retention members 28, 30. Preferably, distance d₄ is less than about 80% such as less than about 70% of d₁. In the insertion state, a distal extent of one and preferably both retention members 28, 30 is preferably greater than a distal extent of rotatable connection 56 of linkage 46. Therefore, when catheter 20 is viewed along central axis a₁ in the insertion state, retention members 28, 30 preferably enclose linkage 46 so that when catheter 20 is inserted, linkage portions 52, 54 do not contact the passage.

In the insertion state, rotation axis a₅ of rotatable connection 56 is preferably distal to rotation axes a₆, a₇ of respective rotatable connections 62, 64. In the retention state, rotation axis a₅ may be proximal to rotation axes a₆, a₇. Preferably, a line between one of rotation axes a₆, a₇ and rotation axis a₅ defines an angle θ₂ of at least about 5 degrees and more preferably at least about 10 degrees with respect to a line normal to central axis a₂ of distal portion 27. Angle θ₂ is preferably less than about 25 degrees, such as less than about 18 degrees. In some embodiments, rotation axis a₅ may be distal to rotation axes a₆, a₇ in the retention state.

In use, an operator may insert catheter 20 along a passage, such as a urethra, until retention members 28, 30 are disposed within a body cavity, such as a bladder. Proximal catheter portion 24 may include one or more radially extending elements 76, which are seen in FIGS. 1 and 2 and prevent over-insertion of catheter 20. Once retention members 28, 30 are disposed within a body cavity, the operator actuates linkage 46 to open the retention members to the retention state. Catheter 20 includes an actuation member 74, which is preferably configured to communicate tension to linkage 46 to actuate the opening motion of retention members 28, 30. In use, actuation member 74 may extend from linkage 46 generally along lumen 32 to proximal portion 24 of catheter 20. An operator may actuate linkage 46 by, for example, applying tension to a proximal portion of actuation member 74. Actuation member 74 may be a filament, fine wire, or other string-like element that may communicate, such as by communicating tension, with linkage 46 for actuation thereof.

Actuation member 74 may extend along the same lumen used to provide drainage of fluid. Alternatively, the elongate body may be provided with a second, preferably separate lumen. Actuation member 74 may extend along this second lumen. In any event, it is preferred that a proximal portion of actuation member 74 be accessible to an operator inserting catheter 20 along a urethra of a patient.

In addition to, or as an alternative to, actuating an opening movement of the retention members, the actuation member 74 may be configured to resist a closing motion of the retention members absent the application of a traumatic withdrawal force to the retained catheter. Preferably, once the retention members have been moved to the retention state in a bladder, actuation member 74 is secured so that a closing motion of the retention members applies increasing tension to the actuation member. For example, referring to FIG. 8, a distal portion of actuation member 74 is secured to linkage 46 adjacent axis a₅ thereof. Upon deployment of the retention members, a proximal portion of the actuation member may be secured, such as to a proximal portion of the elongate body. Axis a₅ is disposed distal to axes a₆ and a₇ in the retention state. A closing motion of the retention members urges linkage 46 distally at axis a₅ thus applying tension to the secured actuation member 74. At least one of the linkage and retention members may include a mechanical stop configured to maintain axis a₅ distally to axes a₆, a₇ in the retention state.

The tension applied to actuation member 74 by linkage 46 resists movement of the linkage and, therefore, the closing motion of the retention members. However, upon the application of a traumatic withdrawing force, the retention members overcome the resistance offered by the actuation member and return to the insertion state allowing injury-free withdrawal.

In one embodiment, the actuation member is elastically secured, preferably to linkage 46 and a proximal portion of the elongate body. For example, the actuation member may itself be elastic. A closing motion of the retention members may stretch the actuation member. A sufficient withdrawal force overcomes the elasticity allowing the retention members to return to the insertion state. Alternatively, or in addition to an elastically secured actuation member, the elongate body may have a degree of compressibility. In this case, a closing motion of the retention members applies tension to the secured actuation member. The tension causes compression of at least a portion of the elongate body. Once the elongate body has compressed sufficiently, linkage 46 is provided with enough freedom of movement to allow the retention members to return to the insertion state.

When retention members 28, 30 are inserted into a body cavity and moved to the retention state, the retention members preferably resist proximal motion of catheter 20 to thereby maintain fluid communication between passage 38 and the body cavity. In use, however, sudden traumatic forces may be applied to an inserted catheter by, for example, a disoriented patient. A traumatic force is a force sufficient to cause injury to the catheterized individual were the catheter not to return to an insertion state. Therefore, retention members 28, 30 of catheter 20 are configured to return to the insertion state upon the application of such a traumatic force so that catheter 20 may withdraw without causing injury.

To achieve both ordinary retention and injury-free traumatic withdrawal of catheter 20, retention members 28, 30 of catheter 20 preferably resist return to the insertion state with an initial degree of resistance and a later degree of resistance. The initial degree of resistance is greater than the later degree of resistance and may be provided by the configuration of linkage 46. For example, upon the application of a force proximally directed along elongate body 22 when catheter 20 is in the retention state, linkage 46 resists the return of retention members 28, 30 to the insertion state when rotation axis a₅ of rotatable connection 56 is proximal to rotation axes a₆, a₇ of respective rotatable connections 62, 64.

When a traumatic force applied proximally along elongate body 22 overcomes the initial degree of resistance, the configuration of the linkage 46 changes, thereby allowing the retention members 28, 30 to return to an insertion state with a minimum of resistance. By return to an insertion state, it is meant that the catheter returns to a state in which the distal portion of the catheter may pass along a passageway without injury to a catheterized mammal. For example, linkage portions 52, 54 may be configured to disengage one another at rotatable connection 56. Such disengagement may be provided by, for example, a ball-and-socket joint in which the ball-like portion is released from the socket upon the application of a traumatic force. Disengagement may also take place at one of rotatable connections 62, 64. As an alternative to disengagement, one or both of linkage members 52, 54 may be configured to bend or fold up in response to a traumatic proximal force so that retention members 28, 30 may close with a minimum of resistance.

In the retention state, retention members 28, 30 preferably resist proximal movement of catheter 20 for proximally applied forces of less than about 12 Newtons, such as less than about 10 Newtons, for example, less than about 8 Newtons, applied to elongate body 22, but return to an insertion state to permit injury free withdrawal of catheter 20 upon application of a force less than about 25 Newtons, such as a force of less than about 20 Newtons, for example, a force of less than about 15 Newtons. For example, a catheter that resists proximal movement of for proximally, applied forces of less than about 12. Newtons but returns to an insertion state upon application of a force of less than about 20 Newtons might remain retained upon application of an 11 Newton force but return to the insertion state upon application of a force of 18 Newtons. Of course, such a catheter would also return to the insertion state upon application of forces greater than 18 Newtons. It is understood that a force of about 4.4 Newtons is equivalent to about 1 pound of force.

In its application or use, a catheter of the invention is preferably inserted so that when the one or more retention members extend radially within a bladder, respective proximal outer surfaces of the one or more extended retention members contact a surface of the bladder thereby inhibiting proximal movement of the catheter. For example, as seen in FIG. 5, retention members 28, 30 include proximal outer surfaces 58, 60 that may contact the bladder. Retention members of preferred catheters are preferably configured to minimize contact with the trigone of the bladder. As understood in the art, the trigone is a generally triangular shaped region of the interior of the bladder. The trigone is bounded by respective lines extending from the urethral orifice at the bladder neck to the urethral orifices and a line extending between the ureteral orifices.

To allow catheter retention with minimal contact with the trigone, catheters of the invention in the retention state preferably have a first radial extent that is greater than a second radial extent of the catheter. For example, retention members 28, 30 of catheter 20 may be retained within a bladder with only minimal or no contact with the trigone. Referring to FIG. 6, a maximum radial dimension d₅ of retention members 28, 30 is greater than a minimum radial dimension d₆ of the distal portion 26 of the catheter 20. For example, the ratio of the dimensions d₅ and d₆ may be at least about 3, such as at least about 4, and for example at least about 5. The minimum radial extent d₆ may be substantially equal to a diameter d₃ of the distal portion 27. When retention members 28, 30 are disposed generally parallel to the coronal plane of a catheterized individual, they essentially avoid contact with the trigone thereby minimizing discomfort to the catheterized individual.

Catheter 20 may include spatial markers indicative of the spatial orientation of retention members 28, 30, when catheter 20 is in a relaxed, substantially untwisted state. The spatial markers allow an operator to determine the orientation of retention members 28, 30 even when these are present within a body cavity. The spatial markers may be the radially extending elements 76, which, when catheter 20 is in the relaxed state, may lie in the same plane as retention members 28, 30, when in the retention state. Indicia, such as surface markings, on proximal portion 24 may also serve as spatial markers. Spatial markers indicia of the spatial orientation of retention members and/or distal portions of catheters of the present invention may be used with any catheter in accordance with the present invention.

During insertion, torsional forces may cause catheter 20 to depart briefly from a relaxed orientation such that distal portion 26 twists with respect to the spatial markers. However, when catheter 20 is inserted according to catheterization procedures generally practiced by one in the art, such as with proper lubrication, catheter 20 will return substantially to the relaxed orientation so that the orientation of the spatial markers are indicative of the orientation of retention members 28, 30. Thus, the operator may insert catheter 20, determine whether retention members 28, 30 are disposed along a desired orientation, such as the coronal plane, and extend the retention members. Markers 76 may be releasably fixed with respect to retention members 28, 30 to maintain the desired orientation of the retention members 28, 30. For example, proximal portion 24 and/or markers 76 may be taped to the anterior surface of the thigh or to the lower abdomen.

Referring to FIGS. 9 and 10, an exemplary embodiment includes a distal portion 126 of a catheter 120 including first and second retention members 128, 130. In the insertion state, as seen in FIG. 9, retention members 128, 130 cooperate to form a distal body 136 having a central axis a₁₁. A distal extent of a distal end 135 of second retention member 130 is greater than a distal extent of a distal end 133 of first retention member 128. When catheter 120 is inserted along a passage, distal end 135 presents a substantially unbroken surface to the passage as retention members 128, 130 progress therealong. Because distal end 135 presents a substantially unbroken surface, forces directed generally against distal end 135 do not tend to urge retention members 128, 130 apart. The distal end 135 preferably obscures or encloses at least a portion of retention member 128 when catheter 120 is viewed along central axis a₁₁.

Retention members 128, 130 of catheter 120 function in accordance with retention members of catheters of the present invention. Thus, in the retention state, as seen in FIG. 10, distal ends 133, 135 are spaced apart so that catheter 120 resists proximal motion when retention members 128, 130 are disposed within a body cavity. Fluid may pass along a lumen 132 of an elongate body 122 of catheter 120. Lumen 132 includes a distal opening 138, which is in fluid contact with the body cavity when the retention members 128, 130 are disposed therein. A proximal portion (not shown) of catheter 120 may be identical to proximal portion 24 of catheter 20 so that fluid may be collected or disposed of. Catheter 120 may include spatial markers so that the retention state orientation of retention members 128, 130 may be determined.

Retention members 128, 130 may be actuated in accordance with catheters of the present invention. Thus, for example, a linkage 146 of catheter 120 includes a rotatable connection 156 at which first and second linkage portions 152, 154 rotate via respect to one another. Linkage portions 152, 154 are preferably rotatably connected with respective retention members 128, 130. Rotatable connections of linkage 146 may be pivots, flexible connections, ball-and-socket joints, or other connection about which two portions may rotate relative to one another.

Referring to FIGS. 11 and 12, a distal portion 226 of a catheter 220 includes first and second retention members 228, 230, which rotate with respect to catheter 220 about respective axes a₂₃, a₂₄. The rotatable association of the retention members 228, 230 is accomplished by respective first and second pivots 242, 244 but may also be accomplished by other rotatable elements such as flexible connections between the retention members and elongate body 222.

In an insertion state, as seen in FIG. 11, retention members 228, 230 cooperate to form a distal body 234 having a central axis a₂₁. Upon a first actuation motion, the retention members 228, 230 move from the insertion state to a retention state, as seen in FIG. 12, in which the retention members are spaced apart so that catheter 220 resists proximal movement when the retention members are disposed in a body cavity. Upon a second actuation motion, the retention members 228, 230 move from the retention state to the insertion state. An actuation motion of a linkage 246 actuates movement of retention members 228, 230 from the insertion state to the retention state. Linkage 246 includes a linkage member 252 having first and second ends 249, 251.

The opening motion of retention members 228, 230 may be actuated by applying tension to linkage member 252, such as by a tension member 274. The tension member 274 preferably extends from an attachment point 261 of the linkage member 252 to the proximal portion of catheter 220. Upon actuation of linkage 246, first linkage member end 249 rotates with respect to retention member 228 about a rotation axis a₂₆ via a rotatable connection, which is a pivot 262. The rotatable connection may also be, for example, a flexible connection or a ball-and-socket connection.

Second retention member 230 includes a captivating channel 263 having first and second ends 265, 267. Upon actuation of linkage 246, second linkage member end 251 slides generally along captivating channel 263 from the first end 265 to the second end 267 thereof. When a radial extent of first and second retention members 228, 230 is sufficient to resist proximal movement along the passage, second linkage member end 251 releasably associates with a stop 269, as shown in FIG. 11, disposed at the second captivating channel end 267. Stop 269 is preferably at least partially complementary in shape to second linkage member end 251. The releasable association of second linkage member end 251 and stop 269 resists a return motion of second linkage member end 252 from second captivating channel end 267 to first captivating end 265. Thus, in the absence of a traumatic proximal force, catheter 220 remains inserted with the retention members disposed in the body cavity. Linkage member 252 and stop 269 may be characterized as a detent.

To reduce unintentional dissociation of second linkage member end 251 and stop 269, it is desirable that a compressive force be exerted generally along linkage member 252 and stop 269. The compressive force preferably increases friction between second linkage member end 251 and stop 269. Thus, absent a traumatic proximal force, second linkage member end 252 and stop 269 remain associated. To achieve the compression, one or both of first and second members 228, 230 may be urged to rotate about respective axes a₃, a₄ as if to return to the insertion state, thereby providing compression along second linkage member 252 between rotatable connection 262 and stop 269.

One or both of the retention members 28, 30 may be urged to rotate toward the insertion state via the expansion of a compressed resilient material or the contraction of a resilient material under tension. For example, a distance d₂₄ between rotational axis a₂₄ and a shoulder 270 of second retention member 230 is greater than a distance d₂₅ between rotational axis a₂₄ and a proximal end 272 of second retention member 230. A distal end 240 of catheter 220 has a shoulder 274 comprising a resilient material such as surgical rubber. As second retention member rotates into the fully opened state, retention member shoulder 270 contacts catheter shoulder 274, thereby compressing shoulder 274. The compression urges second retention member 230 to rotate in the opposite direction about axis a₂₄, thereby applying the compressive force along second linkage member 252.

Application of a traumatic proximal force to catheter 220 causes retention member 228, 230 to return to the insertion state thereby allowing catheter 220 to withdraw along the passage without causing injury. Linkage member 252 may be constructed of resilient material, which allows a bending motion of the linkage member upon the application of a traumatic force. The bending motion causes second linkage member end 251 and stop 269 to disengage. Linkage member 252 may include a portion having a lowered resistance to bending than other portions of the linkage member. Upon the application of a traumatic force, the linkage member 252 preferentially bends at the portion with lowered bending resistance. For example, linkage member 252 has a lowered resistance to bending about a notch 278 than about other portions of the linkage member.

Retention members 228, 230 may be returned to the insertion state by intentionally disengaging second linkage member end 251 and stop 269. Such dissociation may be accomplished by exerting a distally directed force against a portion of linkage member 252. For example, an operator may insert a stylet or trocar generally along the lumen 232 of catheter 220 and press against a midpoint 280 of linkage member 252, which may bend about a shoulder 282 adjacent captivating channel 263. Once the second linkage member end 251 and stop 269 dissociate, retention members 228, 230 return readily to the insertion state allowing the withdrawal of catheter 220.

Referring to FIGS. 13 and 14, a catheter 320 includes an enclosure 321 and at least first and second retention members 328, 330. Retention members 328, 330 may be disposed in at least an insertion state, as seen in FIG. 13, and a retention state, as seen in FIG. 14. An opening motion of retention members 328, 330 is preferably actuated by expansion of the enclosure 321, such as with a fluid, such as a gas or liquid. Saline is a preferred fluid. A closing motion of retention members 328, 330 is preferably actuated by release of fluid from enclosure 321. Upon opening or closing, retention members 328, 330 preferably rotate about rotation axes a₃₃, a₃₄ with respect to catheter 320. Rotatable association of retention members 328, 330 and catheter 320 may be accomplished by, for example, pivots, hinges, flexible connections, socket joints or other rotatable connection. The actuation of retention members using a fluid may be referred to as hydraulic actuation.

Referring also to FIG. 15, a proximal portion 324 of catheter 320 includes a port 323 in fluid communication with a lumen 333, which extends from port 323 to enclosure 321. Port 323 may be any element that allows the introduction of fluid into lumen 333. For example, the fitting may be compatible with a syringe so that the syringe may be used to inject fluid along lumen 333. Fluid entering lumen 333 expands enclosure 321, which expansion exerts a preferably radial force upon retention members 328, 330 to extend them radially. For example, a radial force may be generated when the expanding enclosure contacts surfaces 327, 329 of retention members 328, 330. Once retention members are radially extended within a cavity of a mammal, proximal motion of catheter 320 is thereby inhibited. Proximal portion 324 of catheter 320 may include spatial markers so that retention members 328, 330 may be opened in a known orientation within the cavity, such as in the coronal plane within the bladder of a human.

Enclosure 321 may be expanded upon injection of less than about 2 cubic centimeters of liquid therein. Enclosure 321 preferably has a maximum dimension d₈ that is less than about 3 times, such as less than about 2 times a maximum radial dimension d₄₃ of a distal portion 327 of catheter 320. Therefore, contact of enclosure 321 with inner surfaces of the cavity preferably has essentially no tendency to retain catheter 320 therein. Rather, resistance to proximal motion of catheter 320 is preferably due essentially only to radially expanded retention members. For example, proximal surfaces 358, 360 of retention members 328, 330 may contact the inner surface of the cavity.

Catheter 320 includes a second lumen 332 running substantially along an elongate body 322 of the catheter. Lumen 332 may operate in accordance with lumen 32 of catheter 20, such as to allow urine to exit a bladder of a catheterized human. A distal end 340 of catheter 320 includes an opening 338 to lumen 332. Retention members 328, 330 may also include passages to allow fluid to communicate between the cavity and lumen 332.

An operator may release fluid from enclosure 321, such as by using a syringe to withdraw fluid from lumen 333 or simply by breaking a seal of port 323. Loss of fluid from enclosure 321 allows the enclosure to collapse so that retention members 328, 330 may return to the insertion state. Thus, catheter 320 may be withdrawn along the passage without injury to the catheterized mammal. In the event of traumatic proximal force applied to catheter 320, fluid exits from enclosure 321, such as by collapse or rupture thereof. The fluid release allows catheter 320 to withdraw without injury.

Referring to FIGS. 16 and 17, a catheter 420 includes a distal portion 426 including first and second retention members 428, 430 comprising first and second enclosures 429, 431. In the insertion state seen in FIG. 16, the enclosures 429, 431 are substantially free of added fluid so that the enclosures do not extend radially thereby allowing catheter 420 to be inserted along a passage. In the retention state seen in FIG. 17, the enclosures included added fluid, such as a liquid, which is preferably saline. The fluid expands the enclosures 429, 431 radially, thereby extending retention members 428, 431. Proximal portion 424 of catheter 420 may include spatial markers so that retention members 428, 430 may be extended in a known orientation within the cavity, such as in the coronal plane within the bladder of a human.

A proximal portion 424 of catheter 420 includes a port 423 in fluid communication with a lumen 433, which extends from port 423 to enclosures 429, 431. Port 423 may be identical with port 333 of catheter 320 to allow introduction of fluid, such as a liquid to lumen 433. Lumen 433 may bifurcate and include openings 435 to enclosures 429, 431. Fluid entering lumen 433 enters and expands enclosures 429, 431, which extend radially. Once enclosures 429, 431 of retention members 428, 431 are radially extended within a cavity of a mammal, proximal motion of catheter 420 is thereby inhibited.

Distal portion 426 of catheter 420 includes cavities 447, 449 into which enclosures 429, 431 may collapse when in the insertion state. Respective walls 443, 445 separate cavities 447, 449 from lumen 432. Enclosures 429, 431 may be formed of material such as plastic or other polymer. Enclosures 429, 431 may be secured to catheter 420, such as by using, for example, at least one of friction, adhesives or ultrasonic welding. Expansion from an insertion state to a retention state preferably increases a radial extent of retention members 428, 430 as compared to any increase of a distal extent thereof. For example, the increase in radial extent may be at least 2, at least 3, or even at least 4 times greater than the increase in distal extent.

Catheter 420 includes a second lumen 432 running substantially along an elongate body 422 of the catheter. Lumen 432 may operate in accordance with lumen 32 of catheter 20, such as to allow urine to exit a bladder of a catheterized human. A distal surface 441 of catheter 420 includes an opening 438 to lumen 432. An opening 439 may be provided at a distal end 436 of catheter 420.

Referring to FIGS. 18-20, a catheter retention device 534 is configured to be operatively secured to an elongate body 522 to provide a catheter that may be inserted along a passage of an animal so that the catheter retention device resides within a cavity of the mammal. The elongate body is preferably a flexible member defining at least one lumen 532 therealong. Suitable flexible members include tubing formed of medical grade rubber, plastic or other polymers. Once inserted, the catheter retention device 534 may be moved to a retention state, which resists proximal motion of the associated elongate body along the passage. The retention device 534 is preferably a urinary catheter retention device configured for insertion along a urethra to a bladder of a human.

Retention device 534 includes a base 541, which is associated with a distal end 440 of the elongate body 522. To increase the association of retention device 533 and elongate body 522, a proximal extension 537 of retention device 534 may extend along a lumen 532 of elongate body 522. A distal opening 538 of base 541 allows fluid to pass between the cavity and lumen 532 of elongate body 522. At least one of base 541 and extension 537 may be secured to elongate body 522. For example, catheter retention device 534 may be secured to the elongate body 522 using, for example, at least one of friction, adhesives or ultrasonic welding.

Retention device 534 includes at least first and second retention members 528, 530, which may be similar or identical with other described retention members of catheters in accordance with the present invention. Thus, in the insertion state, retention members 528, 530 form a distal body defining a central axis a₅₁. Retention members 528, 530 are movably associated with retention device 534. Preferably, retention members are rotatably associated with base 441 of retention member device 534 so that, in the retention state, distal ends 533, 535 of retention members 528, 530 extend radially from central axis a₅₁.

Retention members 528, 530 of retention device 534 may be actuated similarly or identically with other described retention members of catheters in accordance with the present invention. For example, retention device 534 may include a linkage 546 having first and second linkage members 552, 554. A tension member 574 may be used to actuate linkage 546 by applying a proximal tension thereto so that retention device moves from an insertion state seen in FIG. 18 to a retention state seen in FIGS. 19 and 20. Retention members of catheter retention devices of the invention are configured to resist proximal motion of the associated catheter in the absence of traumatic proximal forces. In response to a traumatic proximal force, the retention members are configured to return to the insertion state to allow withdrawal with a reduced risk of injury to the catheterized individual.

Referring to FIGS. 21 and 22, a catheter 620 includes a distal portion 626 having a yoke 623, which operably supports a retention member 628. An elongate body 622, which extends proximally from distal portion 626, includes a lumen 632. An opening 638 allows fluid to enter lumen 632, pass therealong, and exit catheter 620 at a proximal portion 624 thereof.

In an insertion state, seen in FIGS. 21 and 22, retention member 628 is generally aligned with a central axis a₆₂ of a distal portion 627 of elongate body 622 and at least partially enclosed by yoke 623. For example, a portion of retention member 628 may be accommodated by a cavity 635 of yoke 623. Thus, catheter 620 may be inserted along a passageway of a mammal until retention member 628 is disposed within a cavity of the mammal. As discussed below, an operator may selective move the retention member 628 to a retention state, in which first and second ends 629, 631 of retention member 628 are spaced apart radially from axis a₆₂ thereby resisting proximal motion of the catheter 620 along the passageway. When retention member is disposed in the retention state in a cavity, such as a bladder, opening 638 is in fluid communication with the cavity so that fluid may exit the cavity through lumen 632 of catheter 620.

Retention member 628 is preferably rotatably associated with yoke 623. For example, retention member 628 may rotate about a pivot point 638 with respect to yoke 623. Pivot point 638 may be aligned with a rotation axis a₆₃ of retention member 728. Thus, in moving between the insertion state and the retention state, retention member 628 may rotate with respect to axis a₆₂ about rotation axis a₆₃, which may be disposed along retention member 628 between first and second ends 629, 631. Axis a₆₃ is preferably but is not required to be disposed substantially central to first and second ends 629, 631.

A tension member 640 may be used to actuate movement of the retention member 628 between the insertion and retention states. Tension member 640 may be secured to retention member 628 at a point 642, which is spaced apart radially from pivot point 638. Thus, when tension is communicated through tension member 640 to retention member 628, the latter rotates about pivot point 638 thereby moving from the insertion state to the retention state. To withdraw catheter 720, a stylet or trocar may be inserted along lumen 632 to push against a distal surface 644 of retention member 628 thereby urging the retention member to return to the insertion state.

Referring to FIGS. 25 and 26, a catheter 720 includes a retention member 728 and an elongate body 722 having a proximal portion 724 and a distal portion 727. A lumen 732 extends generally along elongate body 722. An opening 738 provides passage for fluid to enter lumen 732 at distal portion 727 of elongate body 722 and pass along lumen 732 to proximal portion 724.

Retention member 728 includes first and second ends 729, 731. In an insertion state, shown in FIG. 25, first and second ends 729, 731 are generally aligned with elongate body 722 to allow insertion thereof along a passageway, such as a urethra, of a mammal. First end 729 may be bifurcated so as to include spaced apart end first ends 729 a, 729 b. In a retention state, shown in FIG. 26, first and second ends 729, 731 are radially spaced apart from elongate body 722 to thereby resist proximal movement of catheter 720 along the passageway.

Retention member 728 is associated with distal portion 727 of elongate body 722 by one and preferably at least two tension members 735. Tension members 735 are preferably secured to elongate body 722 and to a medial portion 743 of retention member 728. Tension members 735 are preferably elastic and, in the insertion state, urge retention member 728, via the medial portion 743, toward a distal end 739 of elongate body 722. Because first-ends 729 a, 729 b are preferably arcuate or canted to one side, the action of tension members 735 causes retention member 728 to rotate about a medially disposed axis a₇ thereof. The rotation of retention member 728 draws medial portion 743 further toward a distal end of elongate body 722 thereby causing first and second ends 729, 731 to extend radially from elongate body 722 so that catheter 720 assumes a retention state as shown in FIG. 26. Because the medial portion 743 moves toward the elongate body 722 upon moving from the insertion state to the retention state, an axial distance d₇₁ between the generally medial portion of the retention member and distal end 739 of the elongate body decreases by at least about one half upon moving from the insertion state to the retention state.

To insert or withdraw catheter 720 along a passageway, such as a urethra, an operator may insert a stylet 748 or trocar along lumen 732 of the catheter until a distal end of the stylet 748 or trocar reaches a notch 750 of retention member 728. A distal end 752 of notch is preferably aligned with or distal to medial portion 743. Thus, as stylet 748 presses against distal end 752 of notch 750, retention member 728 assumes an insertion state as shown in FIG. 25 thereby allowing catheter 720 to be inserted or withdrawn along a passageway.

Once the catheter 720 has been inserted along a passageway so that opening 738 of lumen 732 is in fluid contact with a cavity, the operator may remove stylet 748 thereby allowing catheter 720 to return to the retention state.

Referring to FIGS. 27-29, a catheter 820 includes first and second retention members 828, 830 moveably associated therewith. Catheter 820 also includes an elongate body 822, which may have a lumen 832 therethrough in accordance with the elongate bodies of other catheters discussed herein. For example, lumen 832 may provide a passage for fluid from a distal portion 827 of elongate body to a proximal portion of the elongate body. Only a distal portion 827 of elongate body 822 is shown in FIGS. 27-29. It should be understood, however, that elongate body 822 may be similar or identical to elongate bodies of other catheters discussed herein.

Catheter 820 may include a base 841, which is associated with a distal end 840 of the elongate body 822. A proximal extension 837 may extend partially along lumen 832 from base 841. A distal opening 838 of base 841 allows fluid to pass between a body cavity and lumen 832. At least one of base 841 and extension 837 may be secured to elongate body 822. For example, base 841 and/or extension 837 may be secured to the elongate body 822 using, for example, at least one of friction, adhesives or ultrasonic welding.

First and second retention members 828, 830 are preferably rotatably associated with catheter 820. In the embodiment of FIGS. 27-29, retention members 828, 830 are rotatably associated with base 841 by flexible connections 842, 844. Alternatively, the rotatable association may be accomplished by other elements, such as pivots or ball and socket joints.

A linkage member 846 is operatively associated with the first and second retention members 828, 830. In an insertion state, as shown in FIG. 27, the linkage member 846 inhibits the retention members 828, 830 from moving apart as toward a retention state. Linkage member 846 may be actuated by an actuation member 874 to actuate movement of retention members 828, 830 from the insertion state to the retention state. In a retention state, as shown in FIGS. 28, 29, the linkage member 846 inhibits the retention members 828, 830 from moving toward one another as toward an insertion state. Thus, in the retention state, retention members 828, 830 may operate to retain a catheter in a body cavity in accordance with other retention members discussed herein. Preferably, the body cavity is a bladder and retention of the catheter 820 provides fluid contact between the bladder and an opening 838 to lumen 832.

A first linkage end 862 of linkage member 846 is both rotatably and slidably associated with retention member 828. First linkage end 862 may include projections 867 that engage retention member 828, as by engaging a track 869 therealong. A second linkage end 864 of linkage member 846 is both rotatably and slidably associated with retention member 830. Second linkage end 864 may include projections 871 that engage retention member 830, as by engaging a track 873 therealong.

When retention members are disposed in the insertion state shown in FIGS. 27, 28, a projection 847 of linkage member 846 engages a notch 849 of retention member 828 thereby preventing distal ends 833, 835 of retention members 828, 830 from moving apart radially with respect to one another. Actuation of linkage member 846 via actuation member 874 preferably slides linkage member 846 longitudinally with respect to retention members 828, 830 to thereby disengage linkage member projection 847 and retention member notch 849. For example, linkage member 846 may be actuated by applying tension to actuation member 874 thereby sliding linkage member 846 proximally along tracks 869, 873 in the direction of arrows 875 seen in FIG. 27.

Upon disengagement of projection 847 and notch 849, distal retention member ends 833, 835 may move radially with respect to one another toward the retention state shown in FIGS. 28, 29. As distal retention member ends 833, 835 move radially, retention member 828 rotates with respect to first linkage member end 862 and retention member 830 rotates with respect to second linkage member end 864. First and second linkage member ends 862, 864 may continue to slide with respect to retention members 828, 830 as the retention members move toward the retention state.

When in the retention state, as seen in FIGS. 28, 29, projections 867 of first linkage member end 862 engage narrowed portions 877 of tracks 869 and projections 871 of second linkage member end 864 engage narrowed portions 879 of tracks 873. The engagement of projections 867, 871 and respective narrowed portions 877, 879 inhibits linkage member 846 from sliding with respect to retention members 828, 830 thereby inhibiting the retention members from returning to the insertion state. Thus, when retention members 828, 830 are disposed in a body cavity in the retention state, the retention members will be retained in the body cavity absent a traumatic force applied to the retention members.

When in the retention state within a body cavity, linkage member 846 and retention members 828, 830 preferably resist proximal movement of catheter 832 for proximally applied forces of less than about 12 Newtons, such as less than about 10 Newtons, for example, less than about 8 Newtons, applied to elongate body 22, but return to an insertion state to permit injury free withdrawal of catheter 20 upon application of a force less than about 25 Newtons, such as a force of less than about 20 Newtons, for example, a force of less than about 15 Newtons.

Upon application of a traumatic force, return to an insertion state may be facilitated by a disengagement of linkage member 846 and narrowed portions 877, 879 of retention members 828, 830. Alternatively, linkage member 846 may include a weakened portion, which may be a cut 881 partially through the linkage member 846. Upon the application of a traumatic force to catheter 820 in the retention state, linkage member 846 changes shape, such as by folding about cut 881, thereby allowing retention members 828, 830 to move toward the insertion state and withdraw without injury to the catheterized individual. Retention members 828, 830 may also be returned to the insertion state by inserting a trocar or stylet along lumen 832 to disengage first and second ends 862, 864 of linkage member 846 from narrowed portions of retention members 828, 830 and/or to change the shape of linkage member 846, such as by flexing about cut 881.

Referring to FIGS. 30A-31C, a catheter retention device 934 is configured to be operatively secured to an elongate body to provide a catheter that may be inserted along a passage of an animal until the catheter retention device 934 resides within a cavity of the mammal. The elongate body is preferably a flexible member defining at least one lumen therealong. Suitable flexible members include tubing formed of medical grade rubber, plastic or other polymers. Once inserted, the catheter retention device 934 may be moved to a retention state, which resists proximal motion of the associated elongate body along the passage. The retention device 934 is preferably a urinary catheter retention device configured for insertion along a urethra to a bladder of a human.

Retention device 934 includes a base 941, which, in use, is associated with a distal end of the elongate body used with the device. To increase the association of retention device 934 and the elongate body, a proximal extension 937 of retention device 934 may extend along a lumen of the elongate body. A distal opening 938 of base 941 allows fluid, such as urine, to pass between the cavity and the lumen of the elongate body. At least one of base 941 and extension 937 may be secured to the elongate body. For example, catheter retention device 934 may be secured to the elongate body using, for example, at least one of friction, adhesives or ultrasonic welding.

Retention device 934 may include at least a first retention member 928 and, optionally, a second retention member 930, each of which may be similar or identical with other retention members of catheters in accordance with the present invention. Thus, in the insertion state where both retention members are used, retention members 928, 930 may form a distal body defining a central axis ail. Retention members 928, 930 are movably associated with retention device 934. Preferably, retention members are rotatably associated with base 941 of retention member device 934 so that, in the retention state, distal ends 933, 935 of retention members 928, 930 extend radially from central axis a₉₁.

An opening motion of retention members 928, 930 may be actuated hydraulically. In a preferred embodiment, an opening motion of retention members 928, 930 is actuated by expansion of an enclosure 921, such as with a fluid, such as a gas or liquid. Saline solution is a preferred fluid. A closing motion of retention members 928, 930 is preferably actuated by and/or accompanies a release of fluid from enclosure 921. Upon opening or closing, retention members 928, 930 preferably rotate about rotation axes a₉₃, a₉₄ with respect to retention device 934. Rotatable association of retention members 928, 930 and retention device 934 may be accomplished by, for example, pivots, hinges, flexible connections, socket joints, or other rotatable connection. It should be understood that, as an alternative to hydraulic actuation or in combination therewith, the retention members may be actuated by tension and/or compression as applied by an element extending along the elongate body associated with the device 934.

Retention device 934 may include a linkage comprising a linkage member 946 and enclosure 921. When retention device 934 is in the insertion state, linkage member 946 resists an opening motion of retention members 928, 930. For example, in the insertion state, linkage member 946 may be connected to both retention members 928 and 930. In FIG. 30A, linkage member 946 is connected to a portion 947 of retention member 928 and a portion 948 of retention member 930. The connection between linkage member 946 and retention member 928 is preferably stable in that, upon opening, linkage member 946 remains associated with retention member 928. (FIG. 30B). The connection between linkage member 946 and retention member 930 may be in the form of a catch and notch.

During actuation, the connection between the retention members is preferably released or relaxed by an amount sufficient to allow opening of the retention members. In a preferred embodiment, expansion of enclosure 921 releases (or relaxes, the terms are used interchangeably) the connection, preferably by releasing the connection between linkage member 946 and retention member 930. The introduction of fluid to the enclosure 921 expands the enclosure from within an opening 939 of base 941. Enclosure 921 then applies a force directed generally distally against a lower portion 951 of linkage member 946. The force urges a distal linkage member portion 955 against retention member 928 and urges a linkage member portion 949 generally proximally in the general direction of arrow 953. A space 957 between linkage member 946 and retention member 928 may be provided to allow bowing and/or rotation of the linkage member 946. The motion of linkage member portion 949 releases the connection between linkage member 946 and retention member 930 at portion 948 thereof.

Referring also to FIG. 32, a catheter 975 includes retention device 934 and an elongate body 961 having a first lumen 963 in fluidic communication with the opening 939 and enclosure 921. The elongate body 961 may have a second lumen 983 in fluidic communication with opening 938 to allow fluid to drain from a catheterized mammal. The first lumen may extend to a proximal portion 965 of the elongate body so that an operator may introduce fluid to or withdraw fluid from enclosure 921, as desired.

In one embodiment, the first lumen is in fluidic communication with a port 967, such as a LUER LOC connector to which an operator may connect a syringe. Alternatively, or in combination, the first lumen is in fluidic communication with a proximal enclosure 970, which may include at least one of a flexible sack and a balloon. The proximal enclosure 970 and enclosure 921 are in fluidic communication to the extent that the expansion of one of the enclosures preferably accompanies a contraction of the other enclosure. Thus, for example, to actuate opening of the retention members 928, 930, one may apply pressure to the proximal enclosure 970 causing fluid to exit the proximal enclosure 970 and enter the enclosure 921. The fluid communication may be described as hydraulic communication. Enclosures 921 and 970 may each be configured to accommodate between about 0.2 cc and about 3 cc of fluid, for example, between about 0.5 cc and about 2 cc of fluid.

First lumen 963 may include a sheath-like structure, such as a collar movable therealong. During actuation of retention members 928, 930 from the insertion state to the retention state, the sheath-like structure is moved over enclosure 970. Fluid may then be introduced to enclosure 921, such as by a syringe through portion 967. The sheathlike structure prevents expansion of enclosure 970 during actuation. Once retention members are in the retention state, the sheath-like structure may be removed to allow collapse of enclosure 921 and expansion of enclosure 970 upon a traumatic withdrawal force.

FIG. 32 shows proximal enclosure 970 in the expanded state. Enclosure 921, which is not seen in FIG. 32, is in the contracted state.

Enclosure 921 and proximal enclosure 970 may cooperate to allow a closing motion of retention members 928, 930 upon application of a traumatic force to a retained catheter. Preferably, both enclosure 921 and proximal enclosure 970 comprise a balloon. Upon application of a withdrawal force to a retained catheter, retention members 928, 930 are urged together thereby compressing enclosure 921 therebetween. Initially, enclosure 921 resists a closing motion of the retention members. However, if the withdrawal force is a traumatic force, the compression of enclosure 921 results in a collapse thereof and an expansion of proximal enclosure. The compression required to actuate collapse of enclosure 921 may be determined on the basis of Pascal's principle and La Place's law. Thus, one may choose the sizes and materials of enclosure 921 and proximal enclosure to retain the catheter absent a traumatic force but allow withdrawal in the event of a traumatic force.

In the retention state, retention members 928, 930 preferably resist proximal movement of the catheter for proximally applied forces of less than about 12 Newtons, such as less than about 10 Newtons, for example, less than about 8 Newtons, applied to elongate body 22, but return to an insertion state to permit injury free withdrawal of catheter 20 upon application of a force less than about 25 Newtons, such as a force of less than about 20 Newtons, for example, a force of less than about 15 Newtons. For example, a catheter that resists proximal movement for proximally applied forces of less than about 12 Newtons but returns to an insertion state upon application of a force of less than about 20 Newtons might remain retained upon application of an 11 Newton force but return to the insertion state upon application of a force of 18 Newtons. Of course, such a catheter would also return to the insertion state upon application of forces greater than 18 Newtons. It is understood that a force of about 4.4 Newtons is equivalent to about 1 pound of force.

A preferred attachment of enclosure 921 to base 941 allows fluid to pass in and out of enclosure 921 through opening 939 of base 941. Additionally, enclosure 921 should not obstruct drainage of urine through opening 938. FIG. 31A shows that preferred attachment of enclosure 921 to base 941 is made at radially spaced locations 970 and 971 of opening 939.

Referring to FIGS. 31B and 31C it should be understood that a catheter retention mechanism of the present invention may lack one or both of retention members 928, 930. Instead, enclosure 921 may itself retain the catheter when in the expanded state. In this embodiment, enclosure 921 may be configured to accommodate a greater volume of fluid than when used in cooperation with retention members 928, 930. A preferred catheter of the present invention comprises a distal enclosure, such as a balloon, configured to retain the catheter in a bladder of a mammal and a proximal enclosure in hydraulic communication with the distal enclosure. The two enclosures cooperate as described for enclosures 921, 970 in retaining the catheter and allowing withdrawal upon a traumatic withdrawal force.

While various descriptions of the present invention are described above, it should be understood that the various features can be used singly or in any combination thereof. Therefore, this invention is not to be limited to only the specifically preferred embodiments depicted herein. Further, it should be understood that variations and modifications within the spirit and scope of the invention may occur to those skilled in the art to which the invention pertains. Accordingly, all expedient modifications readily attainable by one versed in the art from the disclosure set forth herein that are within the scope and spirit of the present invention are to be included as further embodiments of the present invention. 

1. A urinary drainage catheter composing: an elongate body comprising: a distal portion; a proximal portion; and first and second separate passages therealong; a distal balloon operatively associated with the distal portion of the elongate body; and a proximal balloon operatively associated with the proximal portion of the elongate body, the distal and proximal balloons being in hydraulic communication with one another via the second passage, wherein an expansion of one of the balloons accompanies a contraction of the other of the balloons.
 2. The urinary drainage catheter of claim 1, wherein when the distal portion of the elongate body is disposed in fluid communication with a bladder of a mammal, the first passage allows fluid to exit the bladder.
 3. A sealed enclosure comprising the urinary drainage catheter of claim 1, wherein the catheter is sterile and at least one of the distal and proximal balloons comprises a fluid.
 4. The sealed enclosure of claim 3, wherein the fluid is an aqueous liquid.
 5. A urinary drainage catheter comprising: an elongate member comprising a distal portion, a proximal portion, and a urinary drainage passage therealong; and a hydraulically actuated retention mechanism operatively associated with the distal end of the elongate member, the hydraulically actuated retention mechanism comprising an actuation fluid and at least one retention member rotatably associated with the distal portion of the elongate body, the retention member (i) being free of the actuation fluid and (ii) being hydraulically rotatable between an insertion state and a retention state, the retention state being configured to resist withdrawal of the catheter when the retention member is deployed in the retention state within the bladder, the actuation fluid not entering the retention member upon actuation to the retention state.
 6. The catheter of claim 5, wherein the catheter comprises a proximal portion having at least one spatial marker indicative of an orientation of the retention members.
 7. A urinary drainage catheter for draining fluid from a bladder of a catheterized mammal, comprising: an elongate body, comprising: a distal portion; a proximal portion; and first and second separate passages extending therealong; a distal enclosure operatively associated with the distal portion of the elongate body and having an insertion state and a retention state, the distal enclosure being inflatable from the insertion state to the retention state upon the introduction of an actuation fluid thereto and collapsible from the retention state to the insertion state upon the exit of at least some of the actuation fluid therefrom, wherein, when the distal enclosure is in the retention state within the bladder, the distal enclosure resists withdrawal of the distal portion of the catheter along the urethra and the first passage facilitates drainage of fluid from the bladder; and a fluid release mechanism operatively associated with the proximal portion of the elongate body, the distal enclosure being in hydraulic communication with the fluid release mechanism via the second passage, wherein, when the catheter is subjected to a traumatic withdrawing force directed substantially along the urethra, the release mechanism operates to allow actuation fluid to exit the second passage, whereupon the distal enclosure collapses to the insertion state.
 8. The urinary drainage catheter of claim 7, wherein the fluid release mechanism is external to the urethra when the distal enclosure is disposed within the bladder.
 9. The urinary drainage catheter of claim 7, wherein the fluid release mechanism comprises an expandable enclosure and operation of the fluid release mechanism comprises introduction of fluid to the expandable enclosure from the second passage.
 10. The urinary drainage catheter of claim 9, wherein the expandable enclosure comprises an expandable balloon formed of elastic material.
 11. The urinary drainage catheter of claim 10, wherein the distal enclosure comprises an expandable balloon formed of elastic material.
 12. The urinary drainage catheter of claim 9, wherein the expandable enclosure is an expandable sack formed of flexible material.
 13. The urinary drainage catheter of claim 7, wherein the fluid release mechanism comprises a membrane and actuation of the fluid release mechanism comprises at least one of an increase in an area of the membrane and a rupture of the membrane.
 14. The urinary drainage catheter of claim 13, wherein the membrane has a thickness less than a thickness of the second passage adjacent the membrane.
 15. The urinary drainage catheter of claim 7, wherein the fluid release mechanism comprises a relief valve.
 16. The urinary drainage catheter of claim 15, wherein the valve is a poppet relief valve. 17-34. (canceled)
 35. A method for catheterizing a mammal comprising: providing a catheter, the catheter comprising: an elongate body comprising: a distal portion; a proximal portion; a distal enclosure operatively associated with the distal portion of the elongate body; and a proximal enclosure having at least one flexible wall, the proximal enclosure being in fluidic communication with the distal enclosure; passing the distal portion of the elongate body along at least a portion of the urethra of the mammal, at least a portion of the proximal enclosure remaining outside the urethra; introducing fluid to the distal enclosure by applying pressure to the flexible wall of the proximal enclosure whereupon fluid exits the proximal enclosure and fluid enters and expands the distal enclosure within the bladder of the mammal, wherein the expanded distal enclosure resists withdrawal of the catheter along the urethra of the mammal.
 36. The method of claim 35, wherein the proximal enclosure comprises at least one of a balloon and a flexible sack and applying pressure to the flexible wall comprises squeezing the at least one of the balloon and flexible sack.
 37. The method of claim 35, wherein the catheter is a urinary drainage catheter comprising at least one drainage passage and, upon expansion of the distal enclosure, a distal opening of the at least one drainage passage is disposed in fluidic communication with the bladder.
 38. The method of claim 35, wherein the step of providing a catheter comprises: opening a sealed enclosure enclosing the catheter, wherein, when the catheter is present within the sealed enclosure, at least one of the proximal and distal enclosures comprise an amount of liquid sufficient to expand the distal enclosure by an amount sufficient to resist withdrawal of the catheter from the urethra. 39-52. (canceled) 